BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    COBALT CHROME FEMORAL HEAD SZ 28 3.5MM 12/14 SHORT NECK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JDI·December 15, 2016

    COCR HEAD SHORT NECK DIA28/-3. 5 MM 12/14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDI·May 10, 2016

    BIOMET COBALT-CHROME FEMORAL COMPONENTS

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·March 17, 2017

    COBALT CHROME FEMORAL HEAD

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L.·Product code JDI·August 31, 2017

    STERRAD 100NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·January 11, 2013

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 29, 2010

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 3, 2014

    BIOMET COBALT-CHROME FEMORAL COMPONENTS

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDI·April 7, 2017

    MENTOR MEMORYGEL BOOST BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·June 10, 2024

    MEDULLARY PLUG WITH DRAIN 4

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZN·January 16, 2018